Investigating outcome measures for assessing airway clearance techniques in adults with cystic fibrosis: protocol of a single-centre randomised controlled crossover trial

被引:9
|
作者
Stanford, Gemma [1 ,2 ]
Davies, Jane C. [2 ,3 ]
Usmani, Omar [2 ,4 ]
Banya, Winston [2 ,4 ]
Charman, Susan [5 ]
Jones, Mandy [6 ]
Simmonds, Nicholas J. [1 ,2 ]
Bilton, Diana [7 ]
机构
[1] Royal Brompton Hosp, Adult Cyst Fibrosis, London, England
[2] Imperial Coll London, Natl Heart & Lung Inst, London, England
[3] Royal Brompton Hosp, Paediat Resp Med, London, England
[4] Royal Brompton Hosp, Res & Dev, London, England
[5] Cyst Fibrosis Trust, London, England
[6] Brunel Univ London, Coll Hlth Med & Life Scientists, Dept Hlth Sci, London, England
[7] Royal Brompton Hosp, Resp Med, London, England
基金
美国国家卫生研究院;
关键词
cystic fibrosis; respiratory measurement; LUNG-DISEASE; INDEX; PHYSIOTHERAPY; SPIROMETRY; CHILDREN; WASHOUT; RANGE;
D O I
10.1136/bmjresp-2020-000694
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Introduction Airway clearance techniques (ACTs) are a gold standard of cystic fibrosis management; however, the majority of research evidence for their efficacy is of low standard; often attributed to the lack of sensitivity from outcome measures (OMs) used historically. This randomised controlled trial (RCT) investigates these standard OMs (sputum weight, forced expiratory volume in 1 s) and new OMs (electrical impedance tomography (EIT), multiple breath washout (MBW) and impulse oscillometry (IOS)) to determine the most useful measures of ACT. Methods and analysis This is a single-centre RCT with crossover design. Participants perform MBW, IOS and spirometry, and then are randomised to either rest or supervised ACT lasting 30-60 min. MBW, IOS and spirometry are repeated immediately afterwards. EIT and sputum are collected during rest/ACT. On a separate day, the OMs are performed with the other intervention. Primary endpoint is difference in change in OMs before and after ACT/rest. Sample size was calculated with 80% power and significance of 5% for each OM (target n=64). Ethics and dissemination Ethics approval was gained from the London-Chelsea Research Ethics Committee (reference 16/LO/0995, project ID 154635). Dissemination will involve scientific conference presentation and publication in a peer-reviewed journal.
引用
收藏
页数:8
相关论文
共 50 条
  • [21] Treatment with l-citrulline and metformin in Duchenne muscular dystrophy: study protocol for a single-centre, randomised, placebo-controlled trial
    Patricia Hafner
    Ulrike Bonati
    Daniela Rubino
    Vanya Gocheva
    Thomas Zumbrunn
    Nuri Gueven
    Dirk Fischer
    Trials, 17
  • [22] Early medical therapy for acute laryngeal injury (ALgI) following endotracheal intubation: a protocol for a prospective single-centre randomised controlled trial
    Lowery, Anne S.
    Kimura, Kyle
    Shinn, Justin
    Shannon, Chevis
    Gelbard, Alexander
    BMJ OPEN, 2019, 9 (07):
  • [23] Bladder cancer and exeRcise trAining during intraVesical thErapy-the BRAVE trial: a study protocol for a prospective, single-centre, phase II randomised controlled trial
    Arthuso, Fernanda Z.
    Fairey, Adrian S.
    Boule, Normand G.
    Courneya, Kerry S.
    BMJ OPEN, 2021, 11 (09):
  • [24] EVerT2-needling versus non-surgical debridement for the treatment of verrucae: study protocol for a single-centre randomised controlled trial
    Hashmi, Farina
    Torgerson, David
    Fairhurst, Caroline
    Cockayne, Sarah
    Bell, Kerry
    Cullen, Michelle
    Harrison-Blount, Michael
    BMJ OPEN, 2015, 5 (11):
  • [25] Effects of a partially supervised conditioning programme in cystic fibrosis: an international multi-centre randomised controlled trial (ACTIVATE-CF): study protocol
    Helge Hebestreit
    Larry C. Lands
    Nancy Alarie
    Jonathan Schaeff
    Chantal Karila
    David M. Orenstein
    Don S. Urquhart
    Erik H. J. Hulzebos
    Lothar Stein
    Christian Schindler
    Susi Kriemler
    Thomas Radtke
    BMC Pulmonary Medicine, 18
  • [26] Effects of a partially supervised conditioning programme in cystic fibrosis: an international multi-centre randomised controlled trial (ACTIVATE-CF): study protocol
    Hebestreit, Helge
    Lands, Larry C.
    Alarie, Nancy
    Schaeff, Jonathan
    Karila, Chantal
    Orenstein, David M.
    Urquhart, Don S.
    Hulzebos, Erik H. J.
    Stein, Lothar
    Schindler, Christian
    Kriemler, Susi
    Radtke, Thomas
    BMC PULMONARY MEDICINE, 2018, 18
  • [27] Utility and validity of dynamic chest radiography in cystic fibrosis (dynamic CF): an observational, non-controlled, non-randomised, single-centre, prospective study
    FitzMaurice, Thomas Simon
    McNamara, Paul Stephen
    Nazareth, Dilip
    McCann, Caroline
    Bedi, Ram
    Shaw, Matthew
    Walshaw, Martin
    BMJ OPEN RESPIRATORY RESEARCH, 2020, 7 (01)
  • [28] Non-Invasive Positive airway Pressure thErapy to Reduce Postoperative Lung complications following Upper abdominal Surgery (NIPPER PLUS): protocol for a single-centre, pilot, randomised controlled trial
    Lockstone, Jane
    Boden, Ianthe
    Robertson, Iain K.
    Story, David
    Denehy, Linda
    Parry, Selina M.
    BMJ OPEN, 2019, 9 (01):
  • [29] Effect of electroacupuncture on the incidence of acute stroke after embolisation of intracranial aneurysm: study protocol for a single-centre, double-blinded, randomised controlled trial
    Zhao, Zi-Jian
    Wang, Hang
    Ye, Qian
    Zhang, Zhen-Feng
    Dong, Shi-Yang
    Xu, Yi-Fan
    Li, Jing-Jin
    Yu, Min
    Feng, Feng
    BMJ OPEN, 2025, 15 (03):
  • [30] Effect of stellate ganglion block on perioperative myocardial injury following thoracoscopic surgery for lung cancer (SGBMI): protocol for a single-centre, randomised controlled trial
    Wu, Wei
    Dai, Haofei
    Liu, Meiyun
    Liu, Yang
    Shi, Hong
    BMJ OPEN RESPIRATORY RESEARCH, 2024, 11 (01)